Li Ruilin, Hu Siyi, Chang Yan, Zhang Zhihui, Zha Zhao, Huang Hui, Shen Guodong, Liu Jing, Song Lihua, Wei Wei
Institute of Clinical Pharmacology, Anhui Medical University, Hefei 230032, China.
Key Laboratory of Anti-inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-inflammatory and Immune Medicine, Hefei 230032, China.
Int J Mol Sci. 2016 Apr 15;17(4):563. doi: 10.3390/ijms17040563.
Human epidermal growth factor receptor 2 (HER2) is one of the most studied tumor-associated antigens for cancer immunotherapy. An engineered anti-HER-2 chimeric A21 antibody (chA21) is a chimeric antibody targeted to subdomain I of the HER2 extracellular domain. Here, we report the anti-tumor activity of the novel engineered monoclonal antibody humanized chA21 (HuA21) that targets HER2 on the basis of chA21, and we describe the underlying mechanisms. Our results reveal that HuA21 markedly inhibits the proliferation and migration of HER2-overexpressing breast cancer cells and causes enhanced antibody-dependent cell-mediated cytotoxicity potency against HER2-overexpressing tumor cells. In particular, HuA21, but not trastuzumab (Tra), markedly suppresses growth and enhances the internalization of the antibody in Tra-resistant BT-474 breast cancer cells. These characteristics are highly associated with the intrinsic ability of HuA21 to down-regulate HER2 activation and inhibit the extracellular signal-regulated kinase 1/2 (ERK1/2) and protein kinase B (Akt) signaling pathways. Furthermore, the combination of HuA21 with Tra synergistically enhances the anti-tumor effects in vitro and in vivo and inhibits HER2 activation and the ERK1/2 and Akt signaling pathways. Altogether, our results suggest that HuA21 may represent a unique anti-HER2 antibody with potential as a therapeutic candidate alone or in combination with other anti-HER2 reagents in cancer therapy.
人表皮生长因子受体2(HER2)是癌症免疫治疗中研究最多的肿瘤相关抗原之一。一种工程化抗HER-2嵌合A21抗体(chA21)是靶向HER2细胞外结构域亚结构域I的嵌合抗体。在此,我们报告了基于chA21靶向HER2的新型工程化单克隆抗体人源化chA21(HuA21)的抗肿瘤活性,并描述了其潜在机制。我们的结果显示,HuA21显著抑制HER2过表达乳腺癌细胞的增殖和迁移,并增强对HER2过表达肿瘤细胞的抗体依赖性细胞介导的细胞毒性作用。特别是,HuA21而非曲妥珠单抗(Tra)能显著抑制Tra耐药的BT-474乳腺癌细胞的生长并增强抗体的内化。这些特性与HuA21下调HER2激活以及抑制细胞外信号调节激酶1/2(ERK1/2)和蛋白激酶B(Akt)信号通路的内在能力高度相关。此外,HuA21与Tra联合使用在体外和体内均协同增强抗肿瘤作用,并抑制HER2激活以及ERK1/2和Akt信号通路。总之,我们的结果表明,HuA21可能是一种独特的抗HER2抗体,具有单独或与其他抗HER2试剂联合用于癌症治疗的潜在候选价值。